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Cloning and characterization of an ftsZ homologue from a bacterial symbiont of Drosophila melanogaster
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0003-2697(83)90418-9openalex-snapshot
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/0092-8674(92)90163-7openalex-snapshot
The small GTP-binding protein rho regulates the assembly of focal adhesions and actin stress fibers in response to growth factors
inferredcites →https://doi.org/10.1016/0092-8674(92)90164-8openalex-snapshot
The small GTP-binding protein rac regulates growth factor-induced membrane ruffling
inferredcites →https://doi.org/10.1016/0168-9525(90)90045-8openalex-snapshot
Regulation of cell division in E. coli
inferredcites →https://doi.org/10.1016/0169-5347(90)90121-sopenalex-snapshot
Drosophila: A laboratory handbook
inferredcites →https://doi.org/10.1016/0300-9084(88)90119-8openalex-snapshot
Escherichia coli and Salmonella typhimurium: Cellular and molecular biology
inferredcites →https://doi.org/10.1016/0378-1119(85)90179-9openalex-snapshot
The nucleotide sequence of the essential cell-division gene ftsZ of Escherichia coli
inferredcites →https://doi.org/10.1016/0962-8924(92)90174-lopenalex-snapshot
The small GTP-binding protein rac regulates growth factor-induced membrane ruffling
inferredcites →https://doi.org/10.1016/0965-1748(92)90136-3openalex-snapshot
Phylogeny of symbiotic bacteria of four weevil species (coleoptera: curculionidae) based on analysis of 16S ribosomal DNA
inferredcites →https://doi.org/10.1016/0968-0004(90)90285-jopenalex-snapshot
Drosophila: A laboratory handbook
inferredcites →https://doi.org/10.1017/s0016672300031529openalex-snapshot
Evidence for aWolbachiasymbiont inDrosophila melanogaster
inferredcites →https://doi.org/10.1017/s0031182000022666openalex-snapshot
The Rickettsia,Wolbachia pipientis(gen. et sp.n.) and Associated Inclusions of the Mosquito,Culex pipiens
inferredcites →https://doi.org/10.1038/348178a0openalex-snapshot
Bidirectional incompatibility between conspecific populations of Drosophila simulans
inferredcites →https://doi.org/10.1038/349117a0openalex-snapshot
The GTPase superfamily: conserved structure and molecular mechanism
inferredcites →https://doi.org/10.1038/353440a0openalex-snapshot
Rapid spread of an inherited incompatibility factor in California Drosophila
inferredcites →https://doi.org/10.1038/354161a0openalex-snapshot
FtsZ ring structure associated with division in Escherichia coli
inferredcites →https://doi.org/10.1038/359251a0openalex-snapshot
Escherichia coli cell-division gene ftsZ encodes a novel GTP-binding protein
inferredcites →https://doi.org/10.1038/359254a0openalex-snapshot
The essential bacterial cell-division protein FtsZ is a GTPase
inferredcites →https://doi.org/10.1073/pnas.89.7.2699openalex-snapshot
16S rRNA phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic incompatibility in insects.
inferredcites →https://doi.org/10.1073/pnas.90.3.1053openalex-snapshot
Escherichia coli cell division protein FtsZ is a guanine nucleotide binding protein.
inferredcites →https://doi.org/10.1093/bioinformatics/5.2.151openalex-snapshot
Fast and sensitive multiple sequence alignments on a microcomputer
inferredcites →https://doi.org/10.1093/genetics/124.2.367openalex-snapshot
Cytoplasmically inherited reproductive incompatibility in Tribolium flour beetles: the rate of spread and effect on population size.
inferredcites →https://doi.org/10.1093/nar/12.1part1.387openalex-snapshot
A comprehensive set of sequence analysis programs for the VAX
inferredcites →https://doi.org/10.1098/rspb.1992.0023openalex-snapshot
Molecular identification ofWolbachia, the agent of cytoplasmic incompatibility inDrosophila simulans, and variability in relation with host mitochondrial types
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00531.xopenalex-snapshot
UNIDIRECTIONAL INCOMPATIBILITY BETWEEN POPULATIONS OF DROSOPHILA SIMULANS
inferredcites →https://doi.org/10.1111/j.1570-7458.1988.tb02299.xopenalex-snapshot
Partial cytoplasmic incompatibility between two Australian populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.2983426openalex-snapshot
Rapid and Sensitive Protein Similarity Searches
inferredcites →https://doi.org/10.1128/jb.142.2.615-620.1980openalex-snapshot
Organization of genes in the ftsA-envA region of the Escherichia coli genetic map and identification of a new fts locus (ftsZ)
inferredcites →https://doi.org/10.1128/jb.163.2.615-622.1985openalex-snapshot
Cell shape and division in Escherichia coli: experiments with shape and division mutants
inferredcites →https://doi.org/10.1128/jb.169.1.1-7.1987openalex-snapshot
Analysis of cell division gene ftsZ (sulB) from gram-negative and gram-positive bacteria
inferredcites →https://doi.org/10.1128/jb.170.10.4855-4864.1988openalex-snapshot
Cloning and characterization of Bacillus subtilis homologs of Escherichia coli cell division genes ftsZ and ftsA
inferredcites →https://doi.org/10.1128/jb.172.5.2765-2768.1990openalex-snapshot
FtsZ regulates frequency of cell division in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.173.11.3500-3506.1991openalex-snapshot
ftsZ is an essential cell division gene in Escherichia coli
inferredcites →https://doi.org/10.1128/jb.173.18.5822-5830.1991openalex-snapshot
Cloning and characterization of a Rhizobium meliloti homolog of the Escherichia coli cell division gene ftsZ
inferredcites →https://doi.org/10.1128/jb.174.1.63-70.1992openalex-snapshot
Roles of MinC and MinD in the site-specific septation block mediated by the MinCDE system of Escherichia coli
inferredcites →https://doi.org/10.1146/annurev.ge.24.120190.001341openalex-snapshot
BACTERIAL CELL DIVISION
inferredcites →https://doi.org/10.1146/annurev.genet.33.1.423openalex-snapshot
Bacterial Cell Division
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5281/zenodo.7666539openalex-extracted
Two parthenogenetic millipede species/lines of the genus Poratia Cook & Cook, 1894 (Diplopoda, Polydesmida, Pyrgodesmidae) found free from Wolbachia bacteria
inferred← citeshttps://doi.org/10.1006/jipa.1997.4739openalex-snapshot
Screening Mollusks forWolbachiaInfection
inferred← citeshttps://doi.org/10.1006/jipa.2001.5009openalex-snapshot
The Association of Western Flower Thrips, Frankliniella occidentalis, with a near Erwinia Species Gut Bacteria: Transient or Permanent?
inferred← citeshttps://doi.org/10.1007/978-90-481-2731-3_11openalex-snapshot
Endosymbiotic bacteria living inside the poultry red mite (Dermanyssus gallinae)
inferred← citeshttps://doi.org/10.1007/978-94-009-1535-0_46openalex-snapshot
PCR-based detection and identification of insect symbionts
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Wolbachia: intracellular manipulators of mite reproduction
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Does a parthenogenesis-inducing Wolbachia induce vestigial cytoplasmic incompatibility?
inferred← citeshttps://doi.org/10.1007/s00248-006-9036-xopenalex-snapshot
Closely Related Wolbachia Strains within the Pumpkin Arthropod Community and the Potential for Horizontal Transmission via the Plant
inferred← citeshttps://doi.org/10.1007/s00248-007-9230-5openalex-snapshot
Presence of Wolbachia in Insect Eggs Containing Antimicrobially Active Anthraquinones
inferred← citeshttps://doi.org/10.1007/s00284-002-4010-4openalex-snapshot
Molecular Evidence of Wolbachia Infection in Natural Populations of Tropical Odonates
inferred← citeshttps://doi.org/10.1007/s00284-011-9887-3openalex-snapshot
Detection of Rickettsia and a Novel Haemaphysalis shimoga Symbiont Bacterium in Ticks in Thailand
inferred← citeshttps://doi.org/10.1007/s00284-011-9973-6openalex-snapshot
Survey of Wolbachia and Its Phage WO in the Uzifly Exorista sorbillans (Diptera: Tachinidae)
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Genome organisation and comparative genomics of four novel Wolbachia genome assemblies from Indian Drosophila host
inferred← citeshttps://doi.org/10.1007/s10493-007-9072-3openalex-snapshot
Wolbachia-induced cytoplasmic incompatibility in Japanese populations of Tetranychus urticae (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1007/s10493-008-9230-2openalex-snapshot
Endosymbiotic bacteria living inside the poultry red mite (Dermanyssus gallinae)
inferred← citeshttps://doi.org/10.1007/s10530-015-0985-1openalex-snapshot
Dynamics of infection with Wolbachia in Hypera postica (Coleoptera: Curculionidae) during invasion and establishment
inferred← citeshttps://doi.org/10.1007/s11259-022-09980-xopenalex-snapshot
Spotted fever group Rickettsia, Anaplasma and Coxiella-like endosymbiont in Haemaphysalis ticks from mammals in Thailand
inferred← citeshttps://doi.org/10.1007/s12038-007-0067-3openalex-snapshot
Frequency of infection with A and B supergroup Wolbachia in insects and pests associated with mulberry and silkworm
inferred← citeshttps://doi.org/10.1007/s40858-015-0019-7openalex-snapshot
Fluorescence in situ hybridization analysis of endosymbiont genera reveals novel infection patterns in a tomato-infesting Bemisia tabaci population from Brazil
inferred← citeshttps://doi.org/10.1016/0378-1119(94)90034-5openalex-snapshot
Expression of the division-controlling gene ftsZ during growth and sporulation of the filamentous bacterium Streptomyces griseus
inferred← citeshttps://doi.org/10.1016/0923-2508(96)80290-7openalex-snapshot
Analysis of genes encoding the cell division protein FtsZ and a glutathione synthetase homologue in the cyanobacterium Anabaena sp. PCC 7120
inferred← citeshttps://doi.org/10.1016/j.aspen.2010.12.009openalex-snapshot
Molecular evidence for the presence of the endosymbiontic bacteria Wolbachia in Cotesia populations (Hymenoptera: Braconidae)
inferred← citeshttps://doi.org/10.1016/j.aspen.2016.04.014openalex-snapshot
A prevalence survey of Wolbachia in Polytremis fukia (Lepidoptera: Hesperiidae)
inferred← citeshttps://doi.org/10.1016/s0021-9258(17)31600-9openalex-snapshot
A point mutation converts Escherichia coli FtsZ septation GTPase to an ATPase.
inferred← citeshttps://doi.org/10.1016/s0965-1748(00)00180-6openalex-snapshot
Infection density of Wolbachia and incompatibility level in two planthopper species, Laodelphax striatellus and Sogatella furcifera
inferred← citeshttps://doi.org/10.1016/s0965-1748(98)00119-2openalex-snapshot
Wolbachia infections are distributed throughout insect somatic and germ line tissues
inferred← citeshttps://doi.org/10.1017/cbo9780511542053.010openalex-snapshot
Sex ratio distorters and their detection
inferred← citeshttps://doi.org/10.1017/s000748530999023xopenalex-snapshot
Superinfection of fiveWolbachiain the alnus ambrosia beetle,Xylosandrus germanus(Blandford) (Coleoptera: Curuculionidae)
inferred← citeshttps://doi.org/10.1017/s0007485314000728openalex-snapshot
Host-plant dependent population genetics of the invading weevilHypera postica
inferred← citeshttps://doi.org/10.1017/s0016672300031529openalex-snapshot
Evidence for aWolbachiasymbiont inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1023/a:1006363604916openalex-snapshot
High Temperatures Eliminate Wolbachia, a Cytoplasmic Incompatibility Inducing Endosymbiont, From the Two-spotted Spider Mite
inferred← citeshttps://doi.org/10.1038/45002openalex-snapshot
Germ cells colonized by endosymbiotic bacteria
inferred← citeshttps://doi.org/10.1038/hdy.1997.121openalex-snapshot
Wolbachia and cytoplasmic incompatibility in the spider mites Tetranychus urticae and T. turkestani
inferred← citeshttps://doi.org/10.1038/hdy.2011.82openalex-snapshot
Occasional males in parthenogenetic populations of Asobara japonica (Hymenoptera: Braconidae): low Wolbachia titer or incomplete coadaptation?
inferred← citeshttps://doi.org/10.1038/s41598-021-88770-yopenalex-snapshot
Diversification, selective sweep, and body size in the invasive Palearctic alfalfa weevil infected with Wolbachia
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800329openalex-snapshot
Wolbachia distribution and cytoplasmic incompatibility based on a survey of 42 spider mite species (Acari: Tetranychidae) in Japan
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800605openalex-snapshot
Wolbachia and nuclear–nuclear interactions contribute to reproductive incompatibility in the spider mite Panonychus mori (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800881openalex-snapshot
Cardinium symbionts cause cytoplasmic incompatibility in spider mites
inferred← citeshttps://doi.org/10.1038/sj.hdy.6883850openalex-snapshot
Distribution of Wolbachia among the guild associated with the parthenogenetic gall wasp Diplolepis rosae
inferred← citeshttps://doi.org/10.1038/sj.hdy.6884610openalex-snapshot
Cross-order transfer of Wolbachia from Muscidifurax uniraptor (Hymenoptera: Pteromalidae) to Drosophila simulans (Diptera: Drosophilidae)
inferred← citeshttps://doi.org/10.1046/j.0962-1083.2001.01334.xopenalex-snapshot
Wolbachiainfection shared among planthoppers (Homoptera: Delphacidae) and their endoparasite (Strepsiptera: Elenchidae): a probable case of interspecies transmission
inferred← citeshttps://doi.org/10.1046/j.1365-2583.2000.00203.xopenalex-snapshot
Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty‐three arthropod species
inferred← citeshttps://doi.org/10.1046/j.1365-2672.1999.00476.xopenalex-snapshot
Spacer 2 region and 5S rDNA variation ofWolbachiastrains involved in cytoplasmic incompatibility or sex‐ratio distortion in arthropods
inferred← citeshttps://doi.org/10.1046/j.1365-2915.2000.00202.xopenalex-snapshot
Tissue distribution and prevalence of Wolbachia infections in tsetse flies, Glossina spp.
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1999.00795.xopenalex-snapshot
Acetone preservation: a practical technique for molecular analysis
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2003.01979.xopenalex-snapshot
The distribution and evolutionary history ofWolbachiainfection in native and introduced populations of the invasive argentine ant (Linepithema humile)
inferred← citeshttps://doi.org/10.1046/j.1570-7458.2000.00693.xopenalex-snapshot
Wolbachia‐induced parthenogenesis in the egg parasitoid Telenomus nawai
inferred← citeshttps://doi.org/10.1073/pnas.101304298openalex-snapshot
Removing symbiotic Wolbachia bacteria specifically inhibits oogenesis in a parasitic wasp
inferred← citeshttps://doi.org/10.1073/pnas.222228199openalex-snapshot
Genome fragment of Wolbachia endosymbiont transferred to X chromosome of host insect
inferred← citeshttps://doi.org/10.1073/pnas.91.13.5813openalex-snapshot
GTP-dependent polymerization of Escherichia coli FtsZ protein to form tubules.
inferred← citeshttps://doi.org/10.1073/pnas.94.21.11439openalex-snapshot
The role of Wolbachia bacteria in reproductive incompatibilities and hybrid zones of Diabrotica beetles and Gryllus crickets
inferred← citeshttps://doi.org/10.1080/01647950903431156openalex-snapshot
Evidence of co-specificity betweenTetranychus evansiandTetranychus takafujii(Acari: Prostigmata, Tetranychidae): comments on taxonomic and agricultural aspects
inferred← citeshttps://doi.org/10.1089/104454903321655800openalex-snapshot
Characterization of the ftsZ Gene from Ehrlichia chaffeensis , Anaplasma phagocytophilum , and Rickettsia rickettsii , and Use as a Differential PCR Target
inferred← citeshttps://doi.org/10.1093/genetics/150.1.227openalex-snapshot
Wolbachia Transfer from Drosophila melanogaster into D. simulans: Host Effect and Cytoplasmic Incompatibility Relationships
inferred← citeshttps://doi.org/10.1093/jmedent/37.3.340openalex-snapshot
Distribution and Diversity of Wolbachia Infections in Southeast Asian Mosquitoes (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1093/molbev/msl171openalex-snapshot
A Survey of the Bacteriophage WO in the Endosymbiotic Bacteria Wolbachia
inferred← citeshttps://doi.org/10.1098/rspb.1997.0035openalex-snapshot
Contrasting levels of variability between cytoplasmic genomes and incompatibility types in the mosquitoCulex pipiens
inferred← citeshttps://doi.org/10.1098/rspb.1997.0052openalex-snapshot
Horizontal transmission of parthenogenesis–inducing microbes in Trichogramma wasps
inferred← citeshttps://doi.org/10.1098/rspb.1997.0147openalex-snapshot
Molecular evidence for singleWolbachiainfections among geographic strains of the flour beetleTribolium confusum
inferred← citeshttps://doi.org/10.1098/rspb.1998.0402openalex-snapshot
Evidence for widespread Wolbachia infection in isopod crustaceans: molecular identification and host feminization
inferred← citeshttps://doi.org/10.1098/rspb.1998.0455openalex-snapshot
Successful horizontal transfer of Wolbachia symbionts between Trichogramma wasps
inferred← citeshttps://doi.org/10.1098/rspb.1998.0456openalex-snapshot
Widespread occurrence of the microorganism Wolbachia in ants
inferred← citeshttps://doi.org/10.1098/rspb.2000.1232openalex-snapshot
Wolbachia–induced ‘hybrid breakdown’ in the two–fspotted spider miteTetranychus urticaeKoch
inferred← citeshttps://doi.org/10.1098/rspb.2001.1628openalex-snapshot
Wolbachia–mediated parthenogenesis in the predatory thripsFranklinothrips vespiformis(Thysanoptera: Insecta)
inferred← citeshttps://doi.org/10.1098/rspb.2001.1797openalex-snapshot
Wolbachia–induced parthenogenesis in a genus of phytophagous mites
inferred← citeshttps://doi.org/10.1098/rspb.2009.0313openalex-snapshot
No sex in fungus-farming ants or their crops
inferred← citeshttps://doi.org/10.1099/mic.0.027581-0openalex-snapshot
Extensive genomic diversity of closely related Wolbachia strains
inferred← citeshttps://doi.org/10.1101/2024.03.18.585529openalex-snapshot
Intricate interactions between antiviral immunity and transposable element control in Drosophila
inferred← citeshttps://doi.org/10.1111/ens.12150openalex-snapshot
New haplotype and inter‐strain reproductive compatibility of W olbachia‐uninfected alfalfa weevil, H ypera postica( C oleoptera: C urculionidae), in J apan
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2002.tb00123.xopenalex-snapshot
WOLBACHIA INTERACTIONS THAT DETERMINE DROSOPHILA MELANOGASTER SURVIVAL
inferred← citeshttps://doi.org/10.1111/j.0014-3820.2002.tb01447.xopenalex-snapshot
WITHIN- AND BETWEEN-POPULATION VARIATION FOR WOLBACHIA-INDUCED REPRODUCTIVE INCOMPATIBILITY IN A HAPLODIPLOID MITE
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2010.01556.xopenalex-snapshot
Few parasites, and no evidence for Wolbachia infections, in a freshwater ostracod inhabiting temporary ponds
inferred← citeshttps://doi.org/10.1111/j.1365-2583.1994.tb00160.xopenalex-snapshot
A prokaryotic dnaA sequence in Drosophila melanogasten Wolbachia infection and cytoplasmic incompatibility among laboratory strains
inferred← citeshttps://doi.org/10.1111/j.1365-2583.1995.tb00029.xopenalex-snapshot
PCR‐based detection of Wolbachia , cytoplasmic incompatibility microorganisms, infected in natural populations of Laodelphax striatellus (Homoptera: Delphacidae) in central Japan: has the distribution of Wolbachia spread recently?
inferred← citeshttps://doi.org/10.1111/j.1365-2583.1996.tb00057.xopenalex-snapshot
Molecular identification of a Wolbachia endosymbiont in a Tetranychus urticae strain (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02147.xopenalex-snapshot
Genetic diversity andWolbachiainfection of theDrosophilaparasitoidLeptopilina clavipesin western Europe
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2010.04599.xopenalex-snapshot
Ecology,Wolbachiainfection frequency and mode of reproduction in the parasitoid waspTetrastichus coeruleus(Hymenoptera: Eulophidae)
inferred← citeshttps://doi.org/10.1111/j.1365-2958.1994.tb01285.xopenalex-snapshot
Growth and viability of Streptomyces coelicolor mutant for the cell division gene ftsZ
inferred← citeshttps://doi.org/10.1111/j.1439-0418.2009.01473.xopenalex-snapshot
Life‐cycle variation, including female production by virgin females inFrankliniella occidentalis(Thysanoptera: Thripidae)
inferred← citeshttps://doi.org/10.1111/jbi.12107openalex-snapshot
Reproductive and phylogenetic divergence of tidepool copepod populations across a narrow geographical boundary in Baja California
inferred← citeshttps://doi.org/10.1128/aem.00069-12openalex-snapshot
High-Throughput PCR Assays To Monitor Wolbachia Infection in the Dengue Mosquito (Aedes aegypti) and Drosophila simulans
inferred← citeshttps://doi.org/10.1128/aem.63.10.3926-3932.1997openalex-snapshot
Endosymbionts of ticks and their relationship to Wolbachia spp. and tick-borne pathogens of humans and animals
inferred← citeshttps://doi.org/10.1128/aem.68.2.999-1004.2002openalex-snapshot
Novel Clade of Rickettsia spp. from Leeches
inferred← citeshttps://doi.org/10.1128/aem.69.10.6082-6090.2003openalex-snapshot
Diversity ofWolbachiaEndosymbionts in Heteropteran Bugs
inferred← citeshttps://doi.org/10.1128/aem.71.11.6910-6917.2005openalex-snapshot
Efficient Procedure for Purification of ObligateIntracellular Wolbachia pipientis and RepresentativeAmplification of Its Genome by Multiple-DisplacementAmplification
inferred← citeshttps://doi.org/10.1128/jb.178.5.1320-1327.1996openalex-snapshot
Isolation of an ftsZ homolog from the archaebacterium Halobacterium salinarium: implications for the evolution of FtsZ and tubulin
inferred← citeshttps://doi.org/10.1128/jb.179.14.4545-4552.1997openalex-snapshot
The 75-kilodalton antigen of Bartonella bacilliformis is a structural homolog of the cell division protein FtsZ
inferred← citeshttps://doi.org/10.1128/jb.183.7.2219-2225.2001openalex-snapshot
Determination ofWolbachiaGenome Size by Pulsed-Field Gel Electrophoresis
inferred← citeshttps://doi.org/10.1128/jvi.01071-26openalex-snapshot
Extensive variation in virus-induced patterns of transposable element transcripts in Drosophila
inferred← citeshttps://doi.org/10.1139/g00-061openalex-snapshot
Automictic parthenogenesis in the parasitoidVenturia canescens(Hymenoptera: Ichneumonidae) revisited
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.13.1.395openalex-snapshot
BACTERIAL CELL DIVISION
inferred← citeshttps://doi.org/10.1186/s12862-015-0304-6openalex-snapshot
Polyploidy versus endosymbionts in obligately thelytokous thrips
inferred← citeshttps://doi.org/10.1186/s12866-025-04171-5openalex-snapshot
Two novel rickettsiae (Candidatus Rickettsia isanensis and Candidatus Rickettsia ranongensis) and co-detections of bacteria and protozoa in Amblyomma ticks of reptiles from Thailand
inferred← citeshttps://doi.org/10.1201/9780203009918.ch15openalex-snapshot
Parthenogenesis Associated With Wolbachia
inferred← citeshttps://doi.org/10.1303/aez.2002.379openalex-snapshot
Sensitivity comparison of PCR primers for detecting Wolbachia in spider mites.
inferred← citeshttps://doi.org/10.1303/aez.32.485openalex-snapshot
Wolbachia Having No Effect on Reproductive Incompatibility in Tetranychus kanzawai KISHIDA (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1303/aez.34.391openalex-snapshot
Molecular characterization of Rickettsia sp. in a bruchid beetle, Kytorhinus sharpianus (Coleoptera : Bruchidae)
inferred← citeshttps://doi.org/10.1303/aez.34.551openalex-snapshot
Incompatibility and host plant differences among populations of Tetranychus kanzawai Kishida (Acari : Tetranychidae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0055390openalex-snapshot
The Diversity and Evolution of Wolbachia Ankyrin Repeat Domain Genes
inferred← citeshttps://doi.org/10.1371/journal.pone.0106268openalex-snapshot
Global Genetic Differentiation in a Cosmopolitan Pest of Stored Beans: Effects of Geography, Host-Plant Usage and Anthropogenic Factors
inferred← citeshttps://doi.org/10.1371/journal.pone.0261928openalex-snapshot
Cytoplasmic incompatibility in the semivoltine longicorn beetle Acalolepta fraudatrix (Coleoptera: Cerambycidae) double infected with Wolbachia
inferred← citeshttps://doi.org/10.1554/0014-3820(2002)056[1976:witddm]2.0.co;2openalex-snapshot
WOLBACHIA INTERACTIONS THAT DETERMINE DROSOPHILA MELANOGASTER SURVIVAL
inferred← citeshttps://doi.org/10.1556/aphyt.47.2012.1.15openalex-snapshot
Notes on sex ratio and reproductive modes in field populations of two pest thrips species (Thysanoptera, Thripidae) in Italy
inferred← citeshttps://doi.org/10.1590/s1517-83822011000200046openalex-snapshot
Variations in the sensitivity of different primers for detecting Wolbachia in Anastrepha (diptera: tephritidae)
inferred← citeshttps://doi.org/10.1603/0022-2585-39.4.562openalex-snapshot
Searching forWolbachia(Rickettsiales: Rickettsiaceae) in Mosquitoes (Diptera: Culicidae): Large Polymerase Chain Reaction Survey and New Identifications
inferred← citeshttps://doi.org/10.1603/0022-2585-40.2.230openalex-snapshot
Molecular Evidence for Novel Tick-Associated Spotted Fever Group Rickettsiae from Thailand
inferred← citeshttps://doi.org/10.1603/0022-2585-41.6.1175openalex-snapshot
Phylogenetic Characterization of Wolbachia Symbionts Infecting Cimex lectularius L. and Oeciacus vicarius Horvath (Hemiptera: Cimicidae)
inferred← citeshttps://doi.org/10.1603/0046-225x-37.6.1422openalex-snapshot
First Detection of Wolbachia in Arrhenotokous Populations of Thrips Species (Thysanoptera: Thripidae and Phlaeothripidae) and Its Role in Reproduction
inferred← citeshttps://doi.org/10.1603/ec12328openalex-snapshot
DNA-Based Identification of Spider Mites: Molecular Evidence for Cryptic Species of the Genus Tetranychus (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.18174/121512openalex-snapshot
Trichogramma and its relationship with Wolbachia: Identification of Trichogramma species, phylogeny, transfer and costs of Wolbachia symbionts
inferred← citeshttps://doi.org/10.18174/197514openalex-snapshot
Phylogeny and host-symbiont interactions of thelytoky inducing Wolbachia in Hymenoptera
inferred← citeshttps://doi.org/10.2108/zsj.14.701openalex-snapshot
groE-Homologous Operon of Wolbachia, an Intracellular Symbiont of Arthropods: A New Approach for Their Phylogeny
inferred← citeshttps://doi.org/10.2108/zsj.16.955openalex-snapshot
High Prevalence of Wolbachia in the Azuki Bean Beetle Callosobruchus chinensis (Coleoptera, Bruchidae)
inferred← citeshttps://doi.org/10.2300/acari.7.83openalex-snapshot
Intracellular symbiotes in mites and ticks.
inferred← citeshttps://doi.org/10.3390/insects3010161openalex-snapshot
Insect Sex Determination Manipulated by Their Endosymbionts: Incidences, Mechanisms and Implications
inferred← citeshttps://doi.org/10.4039/n09-801openalex-snapshot
Phylogenetic placement and evidence for horizontal transfer of Wolbachia in Plutella xylostella (Lepidoptera: Plutellidae) and its parasitoid, Diadegma insulare (Hymenoptera: Ichneumonidae)
inferred← citeshttps://doi.org/10.4269/ajtmh.2002.66.103openalex-snapshot
Maternal transmission efficiency of Wolbachia superinfections in Aedes albopictus populations in Thailand.
inferred← citeshttps://doi.org/10.5897/ajb.9000364openalex-snapshot
Molecular diagnosis of Wolbachia endosymbiont from Iranian scorpion Hemiscorpius lepturus using polymerase chain reaction (PCR) amplification of 16S rDNA gene
inferred← citeshttps://doi.org/10.70675/131ed218z9059z4573zbe9cz51797ce2d6f6openalex-snapshot
Caractérisation des interactions entre les défenses antivirales et le contrôle génomique des éléments transposables chez Drosophila
inferred← citeshttps://doi.org/10.70675/26b11b57zf1e3z4503za2d4z888d81527d5eopenalex-snapshot
Apport de l'approche évolutive pour l'étude de l'invasion de l'acarien rouge de la tomate, Tetranychus evansi
inferred← citeshttps://doi.org/10.7287/peerj.5486v0.1/reviews/1openalex-snapshot
Peer Review #1 of "A bioinformatics approach to identifying Wolbachia infections in arthropods (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5486v0.1/reviews/2openalex-snapshot
Peer Review #2 of "A bioinformatics approach to identifying Wolbachia infections in arthropods (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5486v0.1/reviews/3openalex-snapshot
Peer Review #3 of "A bioinformatics approach to identifying Wolbachia infections in arthropods (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5486v0.2/reviews/1openalex-snapshot
Peer Review #1 of "A bioinformatics approach to identifying Wolbachia infections in arthropods (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.5486v0.2/reviews/2openalex-snapshot
Peer Review #2 of "A bioinformatics approach to identifying Wolbachia infections in arthropods (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.5486v0.2/reviews/3openalex-snapshot
Peer Review #3 of "A bioinformatics approach to identifying Wolbachia infections in arthropods (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.5486openalex-snapshot
A bioinformatics approach to identifying Wolbachia infections in arthropods
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.